mRNA Metabolism in Normal and Pathological Cells, CNRS, Université Lyon 1, Villeurbanne, France.
Blood Cells Mol Dis. 2011 Oct 15;47(3):158-65. doi: 10.1016/j.bcmd.2011.07.001. Epub 2011 Aug 11.
Complete loss of protein 4.1R in red blood cell membrane is a very rare condition in humans. We here explore the third case. The morphological and biochemical observations suggested that the proband suffers from homozygous hereditary elliptocytosis. Both parents, who are consanguineous, have an elliptocytosis with no cell fragmentation, typical of a heterozygous 4.1R deficiency with a silent allele. A genomic deletion was found; it encompasses about 50 kb of genomic DNA, and suppresses the two key exons 2 and 4, which contain the two functional AUG translation initiation sites in erythroid and nonerythroid cells. The alternative first exons are intact, hence preserving the transcription potential of the altered gene. Extensive analysis of 4.1R transcripts revealed multiple splicing defects upstream of the deleted sequences. Importantly, we found that most of the transcripts generated from the altered gene are intercepted by the nonsense-mediated mRNA decay mechanism, suggesting that the massive degradation of the mRNA species jeopardizes the production of shortened but functional protein 4.1R from an alternative translation initiation site downstream of the deletion.
红细胞膜蛋白 4.1R 完全缺失在人类中非常罕见。我们在此探讨了第三个病例。形态学和生化观察提示该先证者患有纯合遗传性椭圆形红细胞增多症。其父母是近亲结婚,均患有无细胞碎片的椭圆形红细胞增多症,这是杂合 4.1R 缺乏症的典型表现,存在一个沉默等位基因。发现了一个基因组缺失;它包含约 50 kb 的基因组 DNA,抑制了红细胞和非红细胞中两个关键的外显子 2 和 4,其中包含两个功能性 AUG 翻译起始位点。改变基因的替代第一个外显子完整,因此保留了改变基因的转录潜力。对 4.1R 转录物的广泛分析显示,缺失序列上游存在多个剪接缺陷。重要的是,我们发现,大多数从改变基因产生的转录物都被无意义介导的 mRNA 降解机制拦截,这表明 mRNA 物种的大量降解危及了从缺失下游的替代翻译起始点产生缩短但功能正常的蛋白 4.1R。